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Medicine

Furosemide 100 mg/10 mL injection

Furosemide · Intramuscular, intravenous
Available on requestPrescription onlyUS FDAGeneric name

Furosemide 100 mg/10 mL injection is a generic prescription medicine for intramuscular, intravenous use, made by 12 labelers, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Store at 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 30°C…

Key facts

Active ingredient (INN)
Furosemide
Brand
Sold under the generic name
Strength
100 mg/10 mL
Dosage form
Injection
Route
Intramuscular, intravenous
Packs
10 vials of 10 mL, 25 vials of 10 mL, 5 vials of 10 mL and 17 more
Manufacturers
Gland PharmaIndiaAccord HealthcareIndiaEugiaIndiaMicro LabsIndiaHealthFirstFresenius KabiHospiraMedical Purchasing SolutionsMeitheal PharmaceuticalsSagent Pharmaceuticals
Origin register
US FDA, United States
Storage
Store at 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 30°C (59°F to 86°F). Protect from light.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
C03CA01 Furosemide
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
12 July 2000
Identifiers
RxCUI 1719286, 1719290, 1719291 +2DailyMed set ID 39fd32f2-6bb7-4a65-d298-e48d26bc80c7, ddfc41a9-37d4-49c1-bbf3-969a98cd649c, c5d9b063-e3fe-ec2f-e053-2995a90ab3f2 +15NDC 0409-6102, 0143-9157, 51662-1575 +12Application NDA018667, NDA018267, NDA018902 +7

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

Packs from every labeler of this generic presentation.

PackCodeLabelerMarketed since
10 vial, single-dose in 1 carton / 10 mL in 1 vial, single-dose16729-502-43Accord HealthcareIndia21 April 2021
25 vial in 1 carton / 10 mL in 1 vial55150-324-25EugiaIndia3 May 2019
5 vial, glass in 1 box / 10 mL in 1 vial, glass68083-434-05Gland PharmaIndia1 July 2020
25 vial, glass in 1 box / 10 mL in 1 vial, glass68083-434-25Gland PharmaIndia1 July 2020
25 vial in 1 carton / 10 mL in 1 vial42571-438-85Micro LabsIndia1 March 2026
25 vial in 1 tray / 10 mL in 1 vial63323-280-10Fresenius Kabi12 July 2000
25 vial in 1 tray / 10 mL in 1 vial63323-280-36Fresenius Kabi12 July 2000
25 vial, single-dose in 1 tray / 10 mL in 1 vial, single-dose0409-6102-10Hospira31 March 2005
25 vial, single-dose in 1 tray / 10 mL in 1 vial, single-dose0409-6102-27Hospira19 November 2013
25 vial, single-dose in 1 carton / 10 mL in 1 vial, single-dose71288-203-11Meitheal Pharmaceuticals27 January 2022
25 vial, single-dose in 1 carton / 10 mL in 1 vial, single-dose71288-203-94Meitheal Pharmaceuticals27 January 2022
25 vial in 1 carton / 10 mL in 1 vial25021-311-10Sagent Pharmaceuticals15 March 2021
25 vial in 1 carton / 10 mL in 1 vial25021-320-10Sagent Pharmaceuticals15 July 2025
10 vial, single-dose in 1 carton / 10 mL in 1 vial, single-dose0143-9157-10Hikma Pharmaceuticals19 August 2024
10 mL in 1 vial, single-use51662-1226-1HealthFirst14 September 2018
25 pouch in 1 case / 1 vial, single-use in 1 pouch / 10 mL in 1 vial, single-use51662-1226-3HealthFirst22 April 2022
10 mL in 1 vial51662-1575-1HealthFirst28 June 2021
1 vial, single-dose in 1 bag / 10 mL in 1 vial, single-dose71872-7350-1Medical Purchasing Solutions5 May 2025
1 vial, single-dose in 1 bag / 10 mL in 1 vial, single-dose71872-7380-1Medical Purchasing Solutions11 August 2026
25 vial, single-dose in 1 carton / 10 mL in 1 vial, single-dose83634-302-10Avenacy15 March 2024
25 vial in 1 carton / 10 mL in 1 vial23155-473-44—2 September 2014
50 vial in 1 carton / 10 mL in 1 vial23155-473-45—2 September 2014
25 vial, glass in 1 box / 10 mL in 1 vial, glass31722-311-31—13 December 2024
10 vial in 1 carton / 10 mL in 1 vial70756-620-10—17 December 2022
25 vial in 1 carton / 10 mL in 1 vial70756-620-25—17 December 2022
25 vial in 1 carton / 10 mL in 1 vial73542-103-25—16 June 2025
5 vial, single-dose in 1 box / 10 mL in 1 vial, single-dose36000-065-05—6 February 2014
25 vial, single-dose in 1 box / 10 mL in 1 vial, single-dose36000-284-25—6 February 2014
25 vial, glass in 1 box / 10 mL in 1 vial, glass73043-024-01—10 August 2024
25 pouch in 1 box / 1 vial, glass in 1 pouch / 10 mL in 1 vial, glass51662-1720-3—13 December 2024
1 vial in 1 bag / 10 mL in 1 vial71872-7308-1—31 August 2023
25 vial in 1 carton / 10 mL in 1 vial72603-474-25—1 February 2023
25 vial in 1 carton / 10 mL in 1 vial72603-474-25—15 July 2025
10 mL in 1 vial84549-474-25—10 October 2025

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 1 July 1966Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Alternatives

Other makers and brands of Furosemide 100 mg/10 mL injection.

Compare 1

Other strengths and forms of Furosemide

Clinical summary

Furosemide is a loop diuretic indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome. MedsAcross supplies Furosemide for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Read about Furosemide

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

Need Furosemide 100 mg/10 mL injection for your hospital or patient?

Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.